Yin Changjun, Mohanta Sarajo Kumar, Srikakulapu Prasad, Weber Christian, Habenicht Andreas J R
Institute for Cardiovascular Prevention, Ludwig-Maximilians-University, Munich, Germany; German Centre for Cardiovascular Research (DZHK), Partner Site Munich Heart Alliance, Munich, Germany.
Institute for Cardiovascular Prevention, Ludwig-Maximilians-University , Munich , Germany.
Front Immunol. 2016 Oct 10;7:387. doi: 10.3389/fimmu.2016.00387. eCollection 2016.
Artery tertiary lymphoid organs (ATLOs) are atherosclerosis-associated lymphoid aggregates with varying degrees of complexity ranging from small T/B-cell clusters to well-structured lymph node-like though unencapsulated lymphoid tissues. ATLOs arise in the connective tissue that surrounds diseased arteries, i.e., the adventitia. ATLOs have been identified in aged atherosclerosis-prone hyperlipidemic apolipoprotein E-deficient (ApoE) mice: they are organized into distinct immune cell compartments, including separate T-cell areas, activated B-cell follicles, and plasma cell niches. Analyses of ATLO immune cell subsets indicate antigen-specific T- and B-cell immune reactions within the atherosclerotic arterial wall adventitia. Moreover, ATLOs harbor innate immune cells, including a large component of inflammatory macrophages, B-1 cells, and an aberrant set of antigen-presenting cells. There is marked neoangiogenesis, irregular lymphangiogenesis, neoformation of high endothelial venules, and synthesis of lymph node-like conduits. Molecular mechanisms of ATLO formation remain to be identified though media vascular smooth muscle cells may adopt features of lymphoid tissue organizer-like cells by expressing lymphorganogenic chemokines, i.e., CXCL13 and CCL21. Although these data are consistent with the view that ATLOs participate in primary T- and B-cell responses against elusive atherosclerosis-specific autoantigens, their specific protective or disease-promoting roles remain to be identified. In this review, we discuss what is currently known about ATLOs and their potential impact on atherosclerosis and make attempts to define challenges ahead.
动脉三级淋巴器官(ATLOs)是与动脉粥样硬化相关的淋巴样聚集物,其复杂程度各异,从小的T/B细胞簇到结构良好但无包膜的淋巴结样淋巴组织不等。ATLOs出现在患病动脉周围的结缔组织中,即外膜。在易患动脉粥样硬化的老年高脂血症载脂蛋白E缺陷(ApoE)小鼠中已发现ATLOs:它们被组织成不同的免疫细胞区室,包括单独的T细胞区、活化的B细胞滤泡和浆细胞龛。对ATLO免疫细胞亚群的分析表明,在动脉粥样硬化动脉壁外膜内存在抗原特异性T细胞和B细胞免疫反应。此外,ATLOs含有固有免疫细胞,包括大量炎性巨噬细胞、B-1细胞和一组异常的抗原呈递细胞。存在明显的新生血管形成、不规则的淋巴管生成、高内皮微静脉的新形成以及淋巴结样管道的合成。尽管中膜血管平滑肌细胞可能通过表达淋巴器官生成趋化因子(即CXCL13和CCL21)而具有类淋巴组织组织者样细胞的特征,但ATLO形成的分子机制仍有待确定。虽然这些数据与ATLOs参与针对难以捉摸的动脉粥样硬化特异性自身抗原的原发性T细胞和B细胞反应的观点一致,但其具体的保护或促病作用仍有待确定。在这篇综述中,我们讨论了目前关于ATLOs的已知信息及其对动脉粥样硬化的潜在影响,并试图明确未来面临的挑战。